Local structure and near-infrared emission features of neodymium-based amine functionalized organic/inorganic hybrids

被引:49
作者
Gonçalves, MC
Silva, NJO
Bermudez, VDZ [1 ]
Ferreira, RAS
Carlos, LD
Dahmouche, K
Santilli, CV
Ostrovskii, D
Vilela, ICC
Craievich, AF
机构
[1] Univ Tras Os Montes & Alto Douro, Dept Quim, P-5000911 Vila Real, Portugal
[2] Univ Tras Os Montes & Alto Douro, CQ VR, P-5000911 Vila Real, Portugal
[3] Univ Aveiro, Dept Fis, P-3810193 Aveiro, Portugal
[4] Univ Aveiro, CICECO, P-3810193 Aveiro, Portugal
[5] UNESP, Inst Quim, BR-14800900 Araraquara, Brazil
[6] Univ Sao Paulo, Inst Fis, Sao Paulo, SP, Brazil
[7] Chalmers Univ Technol, Dept Appl Phys, S-41296 Gothenburg, Sweden
关键词
D O I
10.1021/jp052097n
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nd3+-based organic/inorganic hybrids have potential application in the field of integrated optics. Attractive sol-gel derived di-urea and di-urethane cross-linked poly (oxyethylene) (POE)/siloxane hybrids (di-ureasils and di-urethanesils, respectively) doped with neodymium triflate (Nd(CF3SO3)(3)) were examined by Fourier transform mid-infrared (FT-IR), Raman (FT-Raman), Si-29 magic-angle spinning (MAS) nuclear magnetic resonance (NMR) and photoluminescence spectroscopies, and small-angle X-ray scattering (SAXS). The goals of this work were to determine which cation coordinating site of the host matrix (ether oxygen atoms or carbonyl oxygen atoms) is active in each of the materials analyzed, its influence on the nanostructure of the samples and its relation with the photoluminescence properties. The main conclusion derived from this study is that the hydrogen-bonded associations formed throughout the materials play a major role in the hybrids nanostructure and photoluminescence properties.
引用
收藏
页码:20093 / 20104
页数:12
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